Subcutaneous Tarlatamab in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-308)
The primary objective of this study is to evaluate the safety and tolerability of subcutaneous (SC) tarlatamab.
Checked against the public recordLast updated Jun 26, 2026 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Basic Science
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- Amgen
- Interventions being studied
- Drug: Tarlatamab
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * Participants ≥ 18 years of age (or ≥ legal adult age within country if it is older than 18 years) at time of signing informed consent. * Participants with histologically or cytologically confirmed ES-SCLC that progressed or recurred following at least one line of platinum-based anti-cancer therapy for SCLC. Note: Participants with prior treatment for LS-SCLC should have also received another regimen for their recurrent, ES-SCLC disease. * Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1. * Participants must have adequate organ function (cardiac, pulmonary, kidney, and liver). * Participants must be able to have SC injections administered in the abdomen. * Participants without measurable disease or tumor tissue (fresh biopsy or archival) available may be permitted after discussion with and approval by Amgen Medical Monitor. Exclusion Criteria: * Participants that have received prior DLL3 targeted therapy. * Participants with untreated or symptomatic brain metastases or those requiring therapy with steroids. * Note: Participants with asymptomatic brain metastatic lesions are allowed following definitive treatment (Amgen Medical Monitor may approve untreated, asymptomatic brain metastasis if local therapy is not required per investigator judgment). * Participants with leptomeningeal disease. * Participants with baseline oxygen requirement.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- University of Southern California, Norris Comprehensive Cancer CenterLos Angeles, California
- University of Illinois ChicagoChicago, Illinois
- Trinity Health Saint Joseph Mercy Ann ArborAnn Arbor, Michigan
- Avera Cancer InstituteSioux Falls, South Dakota
- University of Texas MD Anderson Cancer CenterHouston, Texas
- Swedish Cancer InstituteSeattle, Washington
- Chris OBrien LifehouseCamperdown, New South Wales
- Calvary Mater Newcastle HospitalWaratah, New South Wales
- The Alfred HospitalMelbourne, Victoria
- Universitair Ziekenhuis GentGhent
- Universitair Ziekenhuis Leuven - Campus GasthuisbergLeuven
- Centre Hospitalier Universitaire de Liege - Sart TilmanLiège
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jun 26, 2026. Always confirm current availability with the study team.